510(k) Report

FDA applicant

Jayco Pharmaceuticals

Mchenry, IL9 decisions1981–19850 recalls

FDA records 9 decisions for Jayco Pharmaceuticals (Mchenry, IL) from 1981 to 1985: 9 510(k) clearances. Most are in product codes FED (Endoscopic Access Overtube…) and FOG (Hood, Oxygen, Infant). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Jayco Pharmaceuticals’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jayco Pharmaceuticals since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jayco Pharmaceuticals by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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